Williams, P D <br/><br/>
Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation.  [electronic resource] 

 -  Bioorganic & medicinal chemistry  Sep 1994 
 - 971-85 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0968-0896 
<br/><br/><label>Standard No.: </label>10.1016/s0968-0896(00)82046-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Camphor--analogs & derivatives<br/>Female<br/>Humans<br/>Kidney--metabolism<br/>Kinetics<br/>Liver--metabolism<br/>Male<br/>Models, Molecular<br/>Molecular Conformation<br/>Molecular Sequence Data<br/>Oxytocin--antagonists & inhibitors<br/>Piperazines--chemical synthesis<br/>Rats<br/>Receptors, Oxytocin--antagonists & inhibitors<br/>Receptors, Vasopressin--drug effects<br/>Structure-Activity Relationship<br/>Sulfonamides--chemical synthesis<br/>Tritium<br/>Uterine Contraction--drug effects<br/>Uterus--metabolism